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Active, not recruiting Phase 2 Interventional Results available

A Phase 2 Study of Cediranib in Combination With Olaparib in Advanced Solid Tumors

ClinicalTrials.gov ID: NCT02498613

Public ClinicalTrials.gov record NCT02498613. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 6:31 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This phase II trial studies cediranib maleate in combination with olaparib in treating patients with solid tumors that have spread to other parts of the body (advanced/metastatic) or cannot be removed by surgery (unresectable), including breast cancer, non-small cell lung cancer, small cell lung cancer, and pancreatic cancer. Cediranib maleate and olaparib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Cediranib maleate may also block the flow of oxygen to the tumor, and may help make the tumor more sensitive to olaparib.

Study identification

NCT ID
NCT02498613
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Enrollment
122 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 30, 2016
Primary completion
Jun 21, 2022
Completion
Apr 9, 2027
Last update posted
Jun 16, 2026

2016 – 2027

United States locations

U.S. sites
14
U.S. states
8
U.S. cities
12
Facility City State ZIP Site status
UC San Diego Moores Cancer Center La Jolla California 92093
University of California Davis Comprehensive Cancer Center Sacramento California 95817
UC San Diego Medical Center - Hillcrest San Diego California 92103
UCSF Medical Center-Mount Zion San Francisco California 94115
Smilow Cancer Center/Yale-New Haven Hospital New Haven Connecticut 06510
Yale University New Haven Connecticut 06520
Moffitt Cancer Center-International Plaza Tampa Florida 33607
Moffitt Cancer Center Tampa Florida 33612
Dana-Farber Cancer Institute Boston Massachusetts 02215
Wayne State University/Karmanos Cancer Institute Detroit Michigan 48201
Weisberg Cancer Treatment Center Farmington Hills Michigan 48334
Vanderbilt University/Ingram Cancer Center Nashville Tennessee 37232
UT MD Anderson Cancer Center Houston Texas 77030
VCU Massey Comprehensive Cancer Center Richmond Virginia 23298

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02498613, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 16, 2026 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02498613 live on ClinicalTrials.gov.

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